Empagliflozin as add-on to linagliptin in a fixed-dose combination in Japanese patients with type 2 diabetes: Glycaemic efficacy and safety profile in a 52-week, randomized, placebo-controlled trial

被引:40
作者
Kawamori, Ryuzo [1 ]
Haneda, Masakazu [2 ]
Suzaki, Keiko [3 ]
Cheng, Gang [4 ]
Shiki, Kosuke [3 ]
Miyamoto, Yuki [3 ]
Solimando, Fernando [5 ]
Lee, Christopher [5 ,6 ]
Lee, Jisoo [5 ]
George, Jyothis [5 ]
机构
[1] Juntendo Univ, Sportol Ctr, Grad Sch Med, Tokyo, Japan
[2] Asahikawa Med Univ, Dept Med, Div Metab & Biosyst Sci, Asahikawa, Hokkaido, Japan
[3] Nippon Boehringer Ingelheim Co Ltd, Tokyo, Japan
[4] Boehringer Ingelheim China Investment Co Ltd, Shanghai, Peoples R China
[5] Boehringer Ingelheim GmbH & Co KG, Ingelheim, Germany
[6] Deva Med Consulting Ltd, Chester, Cheshire, England
关键词
empagliflozin; glycaemic control; linagliptin; phase III study; randomized trial; type; 2; diabetes; COTRANSPORTER; 2; INHIBITORS; DOUBLE-BLIND; CARDIOVASCULAR OUTCOMES; POOLED ANALYSIS; THERAPY; MELLITUS; METFORMIN; MONOTHERAPY; MANAGEMENT; SECRETION;
D O I
10.1111/dom.13352
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: This double-blind, randomized, placebo-controlled trial (ClinicalTrials.gov NCT02453555) evaluated the efficacy and safety of empagliflozin (Empa) 10 or 25 mg as add-on to linagliptin (Lina) 5 mg (fixed-dose combination, Empa/Lina 10/5 or 25/5) in insufficiently controlled Japanese type 2 diabetes patients. Methods: The trial (40 sites; May 2015-March 2017) involved screening 433 adults (>= 20 years) who were treatment-naive or were using one oral antidiabetic drug for >= 12 weeks, which was discontinued at enrolment. Patients with HbA1c 7.5%-10.0% after >= 16 weeks of using Lina (pre-enrolment or during a 16-week, open-label period) and 2 weeks of using placebo (Plc) for Empa/Lina 10/5, plus Lina, were randomized (2:1) to once-daily Empa/Lina 10/5 (n = 182) or Plc/Lina 10/5 (n = 93) for 24 weeks. Patients with HbA1c >= 7.0% at Week 24 received Empa/Lina up-titrated to 25/5 (n = 126) or the corresponding placebo (n = 80), per randomization, from Week 28; 172 Empa/Lina and 84 Plc/Lina patients completed 52 weeks. Results: Change from baseline in HbA1c was greater (P < .0001) with Empa/Lina than with Plc/Lina at Week 24 (primary outcome, -0.93% vs 0.21%; adjusted mean difference, -1.14%) and Week 52 (-1.16% vs 0.06%; adjusted mean difference, -1.22%). More patients with HbA1c < 7.0% and greater decreases in fasting plasma glucose, body weight and systolic blood pressure were seen in the Empa/Lina group than in the Plc/Lina group. Empa/Lina was well tolerated. The adverse events that were more frequent with Empa/Lina were known empagliflozin-associated events (eg, increased urination, increased blood ketones). There were no adjudication-confirmed diabetic ketoacidosis events or lower limb amputations. Conclusions: These results support the notion that empagliflozin-linagliptin in fixed-dose combination is a therapeutic option for Japanese patients with type 2 diabetes.
引用
收藏
页码:2200 / 2209
页数:10
相关论文
共 36 条
[1]   Comparison of HOMA-IR, HOMA-β% and disposition index between US white men and Japanese men in Japan: the ERA JUMP study [J].
Ahuja, Vasudha ;
Kadowaki, Takashi ;
Evans, Rhobert W. ;
Kadota, Aya ;
Okamura, Tomonori ;
El Khoudary, Samar R. ;
Fujiyoshi, Akira ;
Barinas-Mitchell, Emma J. M. ;
Hisamatsu, Takashi ;
Vishnu, Abhishek ;
Miura, Katsuyuki ;
Maegawa, Hiroshi ;
El-Saed, Aiman ;
Kashiwagi, Atsunori ;
Kuller, Lewis H. ;
Ueshima, Hirotsugu ;
Sekikawa, Akira .
DIABETOLOGIA, 2015, 58 (02) :265-271
[2]   COMPARISONS OF TREATMENT PATTERNS FOR TYPE 2 DIABETES MELLITUS (T2DMM) IN JAPAN AND IN THE UNITED STATES [J].
Anabuki, K. ;
De, Irwin ;
Winer, I ;
Iizuka, R. ;
Nishikino, R. ;
Palmer, L. A. .
VALUE IN HEALTH, 2016, 19 (07) :A903-A903
[3]  
[Anonymous], TREATM GUID DIAB 201
[4]  
[Anonymous], JAP MED DAT CTR CLAI
[5]   Long-term treatment with empagliflozin as add-on to oral antidiabetes therapy in Japanese patients with type 2 diabetes mellitus [J].
Araki, E. ;
Tanizawa, Y. ;
Tanaka, Y. ;
Taniguchi, A. ;
Koiwai, K. ;
Kim, G. ;
Salsali, A. ;
Woerle, H. J. ;
Broedl, U. C. .
DIABETES OBESITY & METABOLISM, 2015, 17 (07) :665-674
[6]   Fixed-Dose Combination Antidiabetic Therapy: Real-World Factors Associated with Prescribing Choices and Relationship with Patient Satisfaction and Compliance [J].
Benford, Mike ;
Milligan, Gary ;
Pike, James ;
Anderson, Peter ;
Piercy, James ;
Fermer, Steve .
ADVANCES IN THERAPY, 2012, 29 (01) :26-40
[7]   Update review of the safety of sodium-glucose cotransporter 2 inhibitors for the treatment of patients with type 2 diabetes mellitus [J].
Carlson, Curt J. ;
Santamarina, Marile L. .
EXPERT OPINION ON DRUG SAFETY, 2016, 15 (10) :1401-1412
[8]   Diabetes in Asia Epidemiology, Risk Factors, and Pathophysiology [J].
Chan, Juliana C. N. ;
Malik, Vasanti ;
Jia, Weiping ;
Kadowaki, Takashi ;
Yajnik, Chittaranjan S. ;
Yoon, Kun-Ho ;
Hu, Frank B. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 301 (20) :2129-2140
[9]   Clinical pharmacology of dipeptidyl peptidase 4 inhibitors indicated for the treatment of type 2 diabetes mellitus [J].
Chen, Xiao-Wu ;
He, Zhi-Xu ;
Zhou, Zhi-Wei ;
Yang, Tianxin ;
Zhang, Xueji ;
Yang, Yin-Xue ;
Duan, Wei ;
Zhou, Shu-Feng .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2015, 42 (10) :999-1024
[10]  
D'Alessio D, 2011, DIABETES OBES METAB, V13, P126, DOI 10.1111/j.1463-1326.2011.01449.x